Engineering stress as a motivation for filamentous virus morphology.

IF 2.4 Q3 BIOPHYSICS
Andrew McMahon, Swetha Vijayakrishnan, Hafez El Sayyed, Danielle Groves, Michaela J Conley, Edward Hutchinson, Nicole C Robb
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引用次数: 0

Abstract

Many viruses are pleomorphic in shape and size, with pleomorphism often thought to correlate with infectivity, pathogenicity, or virus survival. For example, influenza and respiratory syncytial virus particles range in size from small spherical virions to filaments reaching many micrometers in length. We have used a pressure vessel model to investigate how the length and width of spherical and filamentous virions can vary for a given critical stress and fluorescence super-resolution microscopy along with image analysis tools to fit imaged influenza viruses to the model. We have shown that influenza virion dimensions fit within the theoretical limits of the model, suggesting that filament formation may be a way to increase an individual virus's volume without particle rupture. We have also used cryoelectron microscopy to investigate influenza and respiratory syncytial virus dimensions at the extrema of the model and used the pressure vessel model to explain the lack of alternative virus particle geometries. Our approach offers insight into the possible purpose of filamentous virus morphology and is applicable to a wide range of other biological entities, including bacteria and fungi.

将工程应力作为丝状病毒形态的动力。
许多病毒的形状和大小具有多形性,多形性通常被认为与病毒的感染性、致病性或存活率有关。例如,流感病毒和呼吸道合胞病毒颗粒的大小不一,有的呈小球形,有的呈长达数微米的丝状。我们使用压力容器模型来研究在给定临界压力下球形和丝状病毒的长度和宽度如何变化,并使用荧光超分辨显微镜和图像分析工具将成像的流感病毒与模型相匹配。我们的研究表明,流感病毒的尺寸符合模型的理论限制,这表明病毒丝的形成可能是增加单个病毒体积而不导致颗粒破裂的一种方法。我们还利用低温电子显微镜研究了流感病毒和呼吸道合胞病毒在模型极值处的尺寸,并利用压力容器模型解释了病毒粒子几何形状缺乏替代性的原因。我们的方法有助于深入了解丝状病毒形态的可能目的,并适用于包括细菌和真菌在内的其他多种生物实体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
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0
审稿时长
75 days
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